Clinical Program Leader Program Manager job Cambridge Massachusetts
Clinical Program Leader Program Manager job Cambridge Massachusetts
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Clinical Program Leader/Program Manager Job


Employer Name: BiotechCrossing SpiderID: 2267887
Location: Cambridge, Massachusetts Date Posted: 6/9/2008
Wage: Category: Biotech
Job Code: 5355124

Job Description:


Description: Will work on large, complex registration programs with a large number of sites and a significant number of patients. Will work with the program Medical Directors to provide input to the clinical development plan (CDP). Uses in-depth knowledge of cardiovascular therapeutic area, TA strategies and operational expertise to oversee the Clinical Development Team (CDT), takes a leadership role in the implementation/execution of the CDP, and participates in the development of clinical trial protocol concept in collaboration with the Clinical Development Team. Takes a broad, strategic leadership role in ensuring the successful development and execution of the Clinical Development Plans; utilizes operational expertise, knowledge of TA strategy and TA scientific input when planning program feasibility, developing strategies for country selections, CRO/ vendors use and evaluations and planning for contingencies. SALARY: Salary commensurate with experience BENEFITS: SALARY: Salary commensurate with experience STATUS: Full Time Company Profile:COMPANY PROFILE: About Biogen Idec: Transforming Discovery into Care With operations across the Americas, Europe, and Asia, Biogen Idec (NASDAQ:BIIB) is one of the world's leading biotechnology companies, creating new standards of care in oncology, neurology, and immunology. Every day, employees of Biogen Idec make a difference in people's lives, through pioneering research and development, manufacturing, and our worldwide commercial capabilities. Learn more at www.biogenidec.com/careers. Biogen Idec is proud to be an equal opportunity employer RUBIO/7671BR/IMDV Job Requirements: Thorough knowledge of GCP, ICH guidelines and regulatory requirements for clinical development; Excellent project management skills, including risk assessment and contingency planning. Also requires excellent leadership, communication, management and organizational skills, along with problem solving, conflict resolution, and team building skills. 5+ years of global drug development with experience managing clinical projects within time, budget, and quality expectations; Must have experience in cardiovascular therapeutic area.

For more information, please click here To visit us at BiotechCrossing.

For further information, please visit us online at http://www.biotechcrossing.com

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Job Criteria:
Start Date:
Position Type: Full-Time Permanent
Years of Experience Required:
Education Required:
Overnight Travel:
Vacation Time:


Contact Information:
Contact Name: - Company Type: Employer
Company: BiotechCrossing
City: Pasadena
State: California
Zip: 91101
Web Site: http://www.biotechcrossing.com

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